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Real-time analysis of RAG complex activity in V(D)J recombination
Author(s) -
Jennifer Zagelbaum,
Noriko Shimazaki,
Zitadel Anne Esguerra,
Go Watanabe,
Michael R. Lieber,
Eli Rothenberg
Publication year - 2016
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1606721113
Subject(s) - synapsis , recombination signal sequences , förster resonance energy transfer , v(d)j recombination , molecular beacon , biophysics , rss , single molecule fret , trimer , biology , recombination , chemistry , dna , fluorescence , recombination activating gene , genetics , physics , nuclear magnetic resonance , gene , computer science , oligonucleotide , dimer , quantum mechanics , operating system
Significance Recombination-activating genes 1 and 2 (RAG1/2) and high mobility group box 1 (HMGB1) create dsDNA breaks at recombination signal sequences (RSSs), initiating the variable, diversity, and joining [V(D)J] recombination pathway for antigen–receptor gene assembly. We have discovered that RAG complex binds and bends RSS DNA at the heptamer, with different binding modes for 12RSS and 23RSS substrates. Our experimentally derived binding kinetics have established that binding, bending, and synapsis precede catalysis. We have also directly observed the dynamics of the synaptic complex, revealing that RAG1/2 bending places the nonamers at nearly perpendicular orientations and that the RAG:12RSS:23RSS synaptic complex is very stable. We provide a kinetic model that integrates physical binding, bending, and synapsis steps of the RAG1/2 pathway.

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